BEUDAMED
    32 results · 44ms · Sources: EU EUDAMED, US FDA

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029205·Ø12mm X 50mm Hybrid Fusion Screw, Gen II

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029236·Ø12mm X 65mm Hybrid Fusion Screw, Gen II

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029526·Ø12MM X 30MM HYBRID FUSION SCREW, SACROFUSE

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029557·Ø12MM X 90MM HYBRID FUSION SCREW, SACROFUSE

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029229·Ø12mm X 60mm Hybrid Fusion Screw, Gen II

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029571·Ø12MM X 110MM HYBRID FUSION SCREW, SACROFUSE

    SacroFuse

    FDA UDI
    SPINEFRONTIER, INC.·00190361029540·Ø12MM X 80MM HYBRID FUSION SCREW, SACROFUSE

    LIFEPAK, MODEL 1000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 80); PROVENT PROFESSIONAL SLEEP APNEA THERAPY (PROVENT 50)

    FDA 510(k)
    FDA Class 2 ·Dental

    Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea

    FDA classification
    FDA Class 2 ·Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea

    Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

    FDA classification
    FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

    Automated External Defibrillators (Non-Wearable)

    FDA classification
    FDA Class 3 ·Automated External Defibrillators (Non-Wearable)